The duration of remission and minimal disease activity after initiation and discontinuation of biological agents in patients with early psoriatic arthritis (data from the all-russian psoriatic arthritis registry)
https://doi.org/10.14412/1995-4484-2019-523-527
Abstract
Remission duration and minimal disease activity (MDA) during treatment with biological agents (BA) and after their discontinuation in patients with early psoriatic arthritis (PsA) have been insufficiently studied.
Objective: to study the timing of the onset and duration of remission and MDA after BA initiation and discontinuation in patients with early PsA, followed up according to the Treat-to-Target (T2T) principles.
Subjects and methods. The investigation enrolled 34 patients (18 men, 16 women) with early PsA who met the CASPAR criteria, had participated in the All-Russian Registry and followed up according to the T2T principles.The patients' mean age was 38±11 years; the duration of PsA and psoriasis was 12.0±10.0 and 89.8±91.1 months, respectively. At the beginning of the follow-up, the median DAS and DAPSA scores were 4.05 [3.72; 5.10] and 33.55[28.34; 41.77], respectively. All the patients were prescribed BAs (adalimumab (n=21), ustekinumab (n=8), certolizumab pegol (n=3) or etanercept (n=2)) in combination with methotrexate. The median therapy duration was 9 [6.5; 15] months. The activity of the disease and efficiency of PsA therapy were evaluated using DAS, DAPSA and the criteria for MDA (tender joint count of ≤1, swollen joint count of ≤1, PASI score ≤1 or BSA ≤3, pain intensity on visual analogue scale (VAS) ≤15 mm, patient's assessment of disease activity on VAS ≤20 mm; HAQ score ≤0.5; enthesitis index ≤1) at the beginning of the investigation and then every 3 months. The number of patients who had achieved remission (DAS <1.6; DAPSA ≤4) or MDA (5 of 7 criteria) during BA therapy at least once during the 24-month follow-up was determined. The absence of remission or MDA at the time of examination was considered to be an exacerbation. The duration of remission and MDA was estimated after BA discontinuation according to the activity indices at the time of examination by a physician every 3 months.
Results and discussion. During the 24-month follow-up, DAS/DAPSA remissions were achieved at least once by 28 (82%)/27 (79%) patients, respectively; and MDA was seen in 28 (82%). The first DAS/DAPSA remission occurred after an average of 4.8±2.2/5.8±3.2 months; MDA – after 4.0±1.9 months. The average DAS/DAPSA remission duration was 9.1±5.0/8.3±5.0 months, respectively, and MDA – 11.0±5.5 months. Seven (21%) patients responded to therapy, but did not achieve neither DAPSA, nor DAS remission and 6 (18%) patients did not have MDA. 8 patients in remission continued to receive BAs until the end of the follow-up. Nineteen patients discontinued therapy for various reasons. After discontinuation of BAs, the physician recorded DAS exacerbation in 11 (55%) patients after an average of 6.5±2.3 months and DAPSA exacerbation in 12 (60%)after 5.8±2.3 months. According to the patient assessment, an exacerbation developed in an average of 3.5±3.4 months after BA discontinuation. A DAS/DAPSA exacerbation was observed in 5 (15%) patients during BA therapy after an average of 11.5±4.7/12.0±4.7 months.
Conclusion. During BA therapy, the majority of patients with early PsA achieved remission and MDA following an average of 5 months after the start of treatment using the T2T strategy. After BA discontinuation, an exacerbation occurs in more than half of patients. Following BA discontinuation, the remission duration recorded by the physician according to the activity indices averages 6 months; the duration of subjective improvement according to the patient assessment was 3 months. With continued BA treatment, 15% were observed to have lost its efficiency after an average of 12 months.
About the Authors
E. Yu. LoginovaRussian Federation
34A, Kashirskoe Shosse, Moscow 115522.
T. V. Korotaeva
Russian Federation
34A, Kashirskoe Shosse, Moscow 115522.
S. I. Glukhova
Russian Federation
34A, Kashirskoe Shosse, Moscow 115522.
E. L. Nasonov
Russian Federation
34A, Kashirskoe Shosse, Moscow 115522; 8, Trubetskaya St., Build. 2, Moscow 119991.
References
1. Nasonov EL, editor. Revmatologiya. Rossiyskie klinicheskie rekomendatsii [Rheumatology. Russian Clinical Recommendations]. Moscow: GEOTAR-Media; 2017. 464 p. (In Russ.).
2. Gossec L, Smolen JS, Ramiro S, et al. European League Against Rheumatism (EULAR) recommendations for the management of psoriatic arthritis with pharmacological therapies: 2015 update. Ann Rheum Dis. 2016;75(3):499-510. doi: 10.1136/annrheumdis-2015-208337
3. Coates LC, Moverley AR, McParland L, et al. Effect of tight control of inflammation in early psoriatic arthritis (TICOPA): a UK multicentre, open-label, randomised controlled trial. Lancet. 2015 Dec 19;386(10012):2489-98. doi: 10.1016/S0140-6736(15)00347-5
4. Korotaeva TV, Loginova EYu, Getiya TS, Nasonov EL. Results of one-year treat-to-target strategy in early psoriatic arthritis: data of an open-label REMARCA study. Terapevticheskiy arkhiv. 2018;90(5):22-9 (In Russ.). doi: 10.26442/terarkh201890522-29
5. Smolen JS, Breedveld F, Burmester G, et al. Treating rheumatoid arthritis to target: 2014 update of recommendations by an international task force. Ann Rheum Dis. 2016;75:3-15. doi: 10.1136/annrheumdis-2015-207524
6. Brandt J, Khariouzov A, Listing J, et al. Six-month results of a double-blind, placebo-controlled trial of etanercept treatment in patients with active ankylosing spondylitis. Arthritis Rheum. 2003;48(6):1667-75. doi: 10.1002/art.11017
7. Cantini F, Niccoli L, Cassarа E, et al. Duration of remission after halving of the etanercept dose in patients with ankylosing spondylitis: a randomized, prospective, long-term, follow-up study. Biologics. 2013;7:1-6. doi: 10.2147/BTT.S31474
8. Fautrel B, Verstappen S, Boonen A. Economic consequences and potential benefits. Best Pract Res Clin Rheumatol. 2011;25:607-24. doi: 10.1016/j.berh.2011.10.001
9. Cantini F, Niccoli L, Nannini C, et al. Frequency and duration of clinical remission in patients with peripheral psoriatic arthritis requiring second-line drugs. Rheumatology (Oxford). 2008;47(6):872-6. doi: 10.1093/rheumatology/ken059
10. Huynh DH, Boyd TA, Etzel CJ, et al. Persistence of low disease activity after tumour necrosis factor inhibitor (TNFi) discontinuation in patients with psoriatic arthritis. RMD Open. 2017;3(1):e000395. doi: 10.1136/rmdopen-2016-000395
11. Araujo EG, Finzel S, Englbrecht M, et al. High incidence of disease recurrence after discontinuation of disease-modifying antirheumatic drug treatment in patients with psoriatic arthritis in remission. Ann Rheum Dis. 2015;74(4):655-60. doi: 10.1136/annrheumdis-2013-204229
12. Chimenti MS, Esposito M, Giunta A, et al. Remission of psoriatic arthritis after etanercept discontinuation: analysis of patients' clinical characteristics leading to disease relapse. Int J Immunopathol Pharmacol. 2013;26(3):833-8. doi: 10.1177/039463201302600333
13. Moverley A, Coates L, Marzo-Ortega H, et al. A feasibility study for a randomised controlled trial of treatment withdrawal in psoriatic arthritis (REmoval of treatment for patients in REmission in psoriatic ArThritis (RETREAT (F)). Clin Rheumatol. 2015;34(8):1407-12. doi: 10.1007/s10067-015-2886-1
14. Gonzalez-Alvaro I, Martinez-Fernandez C, Dorantes-Calderоn B, et al. Spanish Rheumatology Society and Hospital Pharmacy Society Consensus on recommendations for biologics optimization in patients with rheumatoid arthritis, ankylosing spondylitis and psoriatic arthritis. Rheumatol (Oxford). 2015;54(7):1200-9. doi: 10.1093/rheumatology/keu461
15. Ye W, Tucker LJ, Coates LC. Tapering and discontinuation of biologics in patients with psoriatic arthritis with low disease activity. Drugs. 2018 Nov;78(16):1705-15. doi: 10.1007/s40265-018-0994-3
Review
For citations:
Loginova E.Yu., Korotaeva T.V., Glukhova S.I., Nasonov E.L. The duration of remission and minimal disease activity after initiation and discontinuation of biological agents in patients with early psoriatic arthritis (data from the all-russian psoriatic arthritis registry). Rheumatology Science and Practice. 2019;57(5):523-527. (In Russ.) https://doi.org/10.14412/1995-4484-2019-523-527